HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858332Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 22125044, compound
https://huagongshe.com/reaction/1858332
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22125173 | HCID 22125173 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22125044 | HCID 22125044 | 100% |
Reaction Steps
A solution of 180 mg (0.3 mmol) of 2-[3-[3-[3-(2,4-dichlorophenyl)-7-methylthio-2-oxo-3,4-dihydro-2H-pyrimido[4,5-d]pyrimidin-1-yl]-phenyl]-propyl]-isoindole-1,3-dione in 10 ml of dichloromethane was treated with 200 mg (0.6 mmol) of 3-chloroperbenzoic acid (50% w/w water) and the mixture stirred at ambient temperature for 18 hours. 0.1 ml of dimethyl sulfoxide was added. After a further 15 minutes 10 ml of dichloromethane and 20 ml of saturated aqueous sodium bicarbonate were added. The organic phase was dried over magnesium sulfate, filtered and evaporated to give 190 mg (100%) of 2-[3-[3-[3-(2,4-dichlorophenyl)-7-methanesulfonyl-2-oxo-3,4-dihydro-2H-pyrimido[4,5-d]pyrimidin-1-yl]-phenyl]-propyl]-isoindole-1,3-dione as a white solid. [Mass spectrum (ESI) MH+ =636].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06150373 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-3ec9fd6d50b44440b450f6c93040a13d |
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| Source note | uspto-grants-2000_11 |
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